Canonical Allele Identifier: CA2499224267
Gene: RAD51D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.35100999del , CM000679.2:g.35100999del GRCh38
NC_000017.10:g.33428018del , CM000679.1:g.33428018del GRCh37
NC_000017.9:g.30452131del NCBI36
NG_031858.1:g.23875del , LRG_516:g.23875del

Transcript Alleles

HGVS Amino-acid Change
ENST00000586186.3:c.810del ENSP00000468273.3:p.Thr271ProfsTer?
ENST00000587405.6:c.588del ENSP00000466478.2:p.Thr197ProfsTer?
ENST00000590016.6:c.1005del ENSP00000466399.1:p.Thr336ProfsTer?
ENST00000592577.6:c.588del ENSP00000466839.2:p.Thr197ProfsTer?
ENST00000345365.11:c.945del MANE Select ENSP00000338790.6:p.Thr316ProfsTer?
ENST00000335858.11:c.609del ENSP00000338408.6:p.Thr204ProfsTer?
ENST00000345365.10:c.945del ENSP00000338790.6:p.Thr316ProfsTer?
ENST00000394589.8:c.945del ENSP00000378090.4:p.Thr316ProfsTer?
ENST00000460118.6:c.414del ENSP00000464356.2:p.Thr139ProfsTer?
ENST00000586044.5:c.*676del ENSP00000465584.1:n.*676del
ENST00000586210.5:c.*539del ENSP00000465612.1:n.*539del
ENST00000587977.5:c.*685del ENSP00000466587.1:n.*685del
ENST00000588372.5:c.*428del ENSP00000468764.1:n.*428del
ENST00000588594.5:c.*541del ENSP00000465366.1:n.*541del
ENST00000590016.5:c.1005del ENSP00000466399.1:p.Thr336ProfsTer?
ENST00000591723.5:c.372+206del ENSP00000467986.1:n.372+206del
ENST00000592181.1:c.546+206del ENSP00000464799.1:n.546+206del
ENST00000593039.5:c.426+206del ENSP00000466834.1:n.426+206del
NM_001142571.1:c.1005del NP_001136043.1:p.Thr336ProfsTer?
NM_002878.3:c.945del , LRG_516t1:c.945del NP_002869.3:p.Thr316ProfsTer?
NM_133629.2:c.609del NP_598332.1:p.Thr204ProfsTer?
NR_037711.1:n.1082del
NR_037712.1:n.947del
NR_037714.1:n.655+206del
NM_001142571.2:c.1005del NP_001136043.1:p.Thr336ProfsTer?
NM_133629.3:c.609del NP_598332.1:p.Thr204ProfsTer?
NR_037711.2:n.971del
NR_037712.2:n.836del
NM_002878.4:c.945del MANE Select NP_002869.3:p.Thr316ProfsTer?